FDA 510(k)

THERM O DRUG MODEL HT-747

K-Number: K922786 · 1993-01-27

Decision Date1993-01-27

Product CodeLGZ

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

THERM O DRUG MODEL HT-747 is the device name listed in this FDA 510(k) record. The listed applicant is C.F. Electronics, Inc.. It received FDA 510(k) clearance on 1993-01-27 under 510(k) number K922786. The device is classified under product code LGZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THERM O DRUG MODEL HT-747?

THERM O DRUG MODEL HT-747 is a medical device that received FDA 510(k) clearance on 1993-01-27. The listed applicant is C.F. Electronics, Inc.. The 510(k) number is K922786.

When did THERM O DRUG MODEL HT-747 receive FDA 510(k) clearance?

THERM O DRUG MODEL HT-747 received FDA 510(k) clearance on 1993-01-27, under 510(k) number K922786.

Who is the listed applicant for THERM O DRUG MODEL HT-747?

The FDA 510(k) record lists C.F. Electronics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THERM O DRUG MODEL HT-747?

The FDA product code for THERM O DRUG MODEL HT-747 is LGZ.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.